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521.
A series of beta-diketone ligands, R(1)COCH(2)COR(2) [tmhdH (R(1) = R(2) = C(CH(3))(3)); tfacH (R(1) = CF(3); R(2) = CH(3)); hfacH (R(1) = R(2) = CF(3))], in combination with tert-butyl peracetate (t-BuPA), have been investigated as etchant solutions for dissolution of copper metal into carbon dioxide solvent. Copper removal in CO(2) increases in the order tfacH < tmhdH < hfacH. A study of the reactions of the hfacH/t-BuPA etchant solution with metallic copper and zinc was conducted in three solvents: scCO(2) (supercrical CO(2)); hexanes; CD(2)Cl(2). The etchant solution/metallic zinc reaction produced a diamagnetic Zn(II) complex, which allowed NMR identification of the t-BuPA decomposition products as tert-butyl alcohol and acetic acid. Gravimetric analysis of the amount of zinc consumed, together with NMR studies, confirmed the 1:1:2 Zn:t-BuPA:hfacH reaction stoichiometry, showing t-BuPA to be an overall two-electron oxidant for Zn(0). The metal-containing products of the copper and zinc reactions were characterized by elemental analysis, IR spectroscopy, and, as appropriate, NMR spectroscopy and single-crystal X-ray diffraction [trans-M(hfac)(2)(H(2)O)(CH(3)CO(2)H) (1, M = Cu; 2, M = Zn)]. On the basis of the experimental results, a working model of the oxidative dissolution reaction is proposed, which delineates the key chemical variables in the etching reaction. These t-BuPA/hfacH etchant solutions may find application in a CO(2)-based chemical mechanical planarization (CMP) process. 相似文献
522.
Abhijit Mitra Pamela J. Seaton Kraig A. Wheeler 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(9):o581-o582
The title new diquinaldine derivative, C27H24N4, forms molecular assemblies organized by intermolecular quinoline π–π stacking [3.356 (3) and 3.440 (3) Å] and both inter‐ and intramolecular N—H⋯N hydrogen bonds [3.039 (3)–3.104 (3) Å and 129 (2)–172 (2)°]. The combination of such interactions provides readily definable contacts that propagate along each crystallographic axis. 相似文献
523.
Peter P. Policastro Pamela K. Hernandez 《Journal of polymer science. Part A, Polymer chemistry》1987,25(10):2819-2826
Alternating polydimethylsiloxane-polyamide block copolymers were prepared in dichloromethane or chloroform solution at room temperature from 3-amino-n-propyl-terminated polydimethylsiloxane oligomers and 2,2′-p-phenylenebis(4,4-dimethyl-5-oxazolone). Solution and thermal properties of the polymers were characterized. 相似文献
524.
Riggs-Gelasco PJ Price JC Guyer RB Brehm JH Barr EW Bollinger JM Krebs C 《Journal of the American Chemical Society》2004,126(26):8108-8109
The Fe(II)- and alpha-ketoglutarate-dependent dioxygenases catalyze hydroxylation reactions of considerable biomedical and environmental significance. Recently, the first oxidized iron intermediate in the reaction of a member of this family, taurine:alpha-ketoglutarate dioxygenase (TauD), was detected and shown to be a high-spin Fe(IV) complex. In this study we have used X-ray absorption spectroscopy to demonstrate the presence of a short (1.62 A) interaction between the iron and one of its ligands in the Fe(IV) intermediate but not in the Fe(II) starting complex. The detection of this interaction strongly corroborates the hypothesis that the intermediate contains an Fe=O structural motif. 相似文献
525.
Molecular force spectroscopy was used to study the mechanical behavior of plasma fibronectin (FN) on mica, gold, poly(ethylene glycol), and -CH(3), -OH, and -COOH terminated alkanethiol self-assembled monolayers. Proteins were examined at two concentrations, one resulting in a saturated surface with multiple intermolecular interactions referred to as the aggregate state and another resulting in a semiaggregate state where the proteins were neither completely isolated nor completely aggregated. Modeling of the force-extension data using two different theories resulted in similar trends for the fitted thermodynamic parameters from which insight into the protein's binding state could be obtained. Aggregated proteins adsorbed on hydrophobic surfaces adopted more rigid conformations apparently as a result of increased surface denaturation and tighter binding while looser conformations were observed on more hydrophilic surfaces. Studies of FN in a semiaggregate state showed heterogeneity in the model's thermodynamic parameters suggesting that, in the early stages of nonspecific adsorption, multiple protein conformations exist, each having bound irreversibly to the substrate. Proteins in this state all demonstrated a more rigid conformation than in the corresponding aggregate studies due to the greater number of substrate contacts available to the protein. Finally, the force spectroscopy experiments were examined for any biocompatibility correlation by seeding substrates with human umbilical vascular endothelial cells. As predicted from the models used in this work, surfaces with aggregated FN promoted cellular deposition while surfaces with FN in a semiaggregate state appeared to hinder cellular deposition and growth. The atomic force microscope's use as a means for projecting surface biocompatibility, although requiring additional testing, does look promising. 相似文献
526.
The structure and properties of electrodeposited poly(vinylferrocene) (PVF) films on platinum electrodes (PVF/Pt) were examined by electron microscopy, X-ray photoelectron spectroscopy, various electrochemical techniques and measurements of the film resistance. The data were consistent with a mechanism in which the polymer films are permeable to dis-solved reactants. A theoretical treatment of this situation for chronoamperometry is presented. The oxidation and reduction of a variety of dissolved reactants with redox potentials far removed from that of the PVF/PVF+ system at PVF/Pt occurred by diffusion of the electroactive species through the polymer film and subsequent reaction at the platinum surface. 相似文献
527.
Biau-Hung Chang Pamela C. Coil Mary J. Brown Kenneth W. Barnett 《Journal of organometallic chemistry》1984,270(1):c23-c25
The compound hydrido cyclopentadienyliron dicarbonyl has been shown by infrared and proton NMR to be present in substantial quantities during hydroformylation of propene and 1-pentene in the presence of [(η5-C5H5)Fe(CO)2]2. This and related observations strongly suggest that the hydride is an important link in the catalytic cycle as is HCo(CO)4 in Co2(CO)8-catalyzed olefin hydroformylation. 相似文献
528.
529.
530.
Zhongyu Wu Zhichao Lin Pamela Mackill Cong Wei John Noonan James Cherniack Deborah Gillis-Landrum 《Journal of Radioanalytical and Nuclear Chemistry》2009,282(3):971-977
Measurement capability and data comparability are essential for emergency response when analytical data from cooperative laboratories
are used for risk assessment and post incident decision making. In this study, the current capability of food emergency response
laboratories for the analysis of 210Po in water was evaluated using a proficiency test scheme in compliance with ISO-43 and ILAC G13 guidelines, which comprises
a test sample preparation and verification protocol and an insightful statistical data evaluation. The results of performance
evaluations on relative bias, value trueness, precision, false positive detection, minimum detection limit, and limit of quantification,
are presented. 相似文献